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PerioChip
PerioChip - 52096-001-22 - (Chlorhexidine Gluconate)
Drug Information of PerioChip
| Product NDC: | 52096-001 |
| Proprietary Name: | PerioChip |
| Non Proprietary Name: | Chlorhexidine Gluconate |
| Active Ingredient(s): | 2.5 mg/1 & nbsp; Chlorhexidine Gluconate |
| Administration Route(s): | PERIODONTAL |
| Dosage Form(s): | INSERT, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of PerioChip
| Product NDC: | 52096-001 |
| Labeler Name: | Adrian Pharmaceuticals, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020774 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19980501 |
Package Information of PerioChip
| Package NDC: | 52096-001-22 |
| Package Description: | 2 BLISTER PACK in 1 CARTON (52096-001-22) > 20 INSERT, EXTENDED RELEASE in 1 BLISTER PACK |
NDC Information of PerioChip
| NDC Code | 52096-001-22 |
| Proprietary Name | PerioChip |
| Package Description | 2 BLISTER PACK in 1 CARTON (52096-001-22) > 20 INSERT, EXTENDED RELEASE in 1 BLISTER PACK |
| Product NDC | 52096-001 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Chlorhexidine Gluconate |
| Dosage Form Name | INSERT, EXTENDED RELEASE |
| Route Name | PERIODONTAL |
| Start Marketing Date | 19980501 |
| Marketing Category Name | NDA |
| Labeler Name | Adrian Pharmaceuticals, LLC |
| Substance Name | CHLORHEXIDINE GLUCONATE |
| Strength Number | 2.5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Decreased Cell Wall Integrity [PE] |
